Trial Search Results

Combination Study Of SB-485232 (Interleukin 18) And Doxil For Advanced Stage Epithelial Ovarian Cancer

The purpose of this study is to identify a dose of SB-485232 which is safe, tolerable and biologically active when used in combination with pegylated liposomal doxorubicin (Doxil) in patients with epithelial ovarian cancer. This study will use a standard treatment regimen of pegylated liposomal doxorubicin (Doxil) in combination with rising doses of SB-485232. The dose selected from this study will be used in a future studies to evaluate the efficacy of this combination.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:


Stanford Investigator(s):


  • Drug: SB-485232 (interleukin 18), pegylated liposomal doxorubicin


Phase 1


Inclusion Criteria:

   1. Female, age ≥18 years of age;

   2. Histologically confirmed diagnosis of epithelial ovarian, fallopian tube, or primary
   peritoneal carcinoma;

   3. Candidate to receive pegylated liposomal doxorubicin for treatment of advanced stage
   ovarian cancer as per standard of care and in the opinion of the treating principal

   4. Measurable lesion(s) according to RECIST v1.0;

   5. ECOG performance status of 0, 1 or 2;

   6. Predicted life expectancy of ≥4 months

   7. No chemotherapy, immunotherapy, hormonal therapy, or biological therapy for cancer,
   radiotherapy, or surgical procedures (except for minor surgical procedures) within
   four weeks before beginning treatment with SB-485232 (six weeks for nitrosoureas and
   mitomycin C). Subjects must have recovered from toxicities (incurred as a result of
   previous therapy) sufficiently to be entered into a Phase I study;

   8. Disease-free period of at least five years from prior malignancies (except for
   curatively treated basal and squamous cell carcinomas of the skin and/or carcinoma of
   the cervix in situ);

   9. Left ventricular ejection fraction (LVEF) ≥50 % as determined by MUGA scan;

10. A signed and dated written informed consent form is obtained from the subject;

11. The subject is able to understand and comply with protocol requirements, timetables,
   instructions and protocol-stated restrictions;

12. The subject is likely to maintain good venous blood access for PK and PD sampling
   throughout the study;

13. A female is eligible to enter and participate in the study if she is of:
   non-childbearing potential (i.e., physiologically incapable of becoming pregnant) or,
   childbearing potential, has a negative serum pregnancy test at the screening visit,
   and agrees to one of several GSK acceptable contraceptive methods;

14. Adequate organ function defined as: ANC ≥1.5 x 10^9/L; hemoglobin ≥9 g/dL (after
   transfusion if needed); platelets ≥75 x 10^9/L.

Exclusion Criteria:

   1. Significant cardiac, pulmonary, metabolic, renal, hepatic, gastrointestinal or
   autoimmune conditions that in the opinion of the investigator and/or GSK medical
   monitor, places the subject at an unacceptable risk as participant in this trial;

   2. Any severe concurrent disease or condition, including significant active autoimmune
   diseases such as rheumatoid arthritis, which in the judgment of the principal
   investigator, would make the subject inappropriate for study participation;

   3. History of myocardial infarction, unstable angina, or acute coronary syndrome within
   the past six months;

   4. The subject has a history of hypersensitivity reactions to a conventional formulation
   of doxorubicin HCl or the components of pegylated liposomal doxorubicin;

   5. The subject has a history of receiving a total cumulative dosage of doxorubicin HCl
   exceeding the currently recommended limit of 550 mg/m^2 or will exceed the 550 mg/m^2
   dosage limit during the course of the current study. A subject will also be excluded
   if they received a lower cumulative dosage of doxorubicin HCl (i.e., 400 mg/m^2) and
   also had prior radiotherapy to the mediastinal area or concomitant therapy with other
   potentially cardiotoxic agents such as cyclophosphamide. Prior use of other
   anthracyclines or anthracenediones should be included in calculations of total
   cumulative doxorubicin HCl dosage;

   6. Women who are pregnant or are breast-feeding;

   7. Corrected QT interval (QTc) ≥480 msec (average of three measurements to be made at

   8. The subject has diabetes mellitus with poor glycemic control;

   9. The subject has a history of human immunodeficiency virus (HIV) or other
   immunodeficiency disease;

10. The subject has positive Hepatitis B surface antigen;

11. The subject has a history of a severe infusion-related reaction following treatment
   with pegylated liposomal doxorubicin as described in the protocol;

12. The subject has an acute infection or severe or uncontrolled infections requiring
   systemic antibiotic therapy;

13. Any serious medical or psychiatric disorder that would interfere with subject safety
   or informed consent;

14. Psychological, familial, sociological, or geographical conditions that do not permit
   compliance with the protocol;

15. Known leptomeningeal disease or evidence of prior or current metastatic brain disease.
   Routine screening with central nervous system (CNS) imaging studies (CT or MRI) is
   required only if clinically indicated;

16. Receiving concurrent chemotherapy, immunotherapy, radiotherapy, or investigational

17. Oral corticosteroids within 14 days of study entry;

18. History of ventricular arrhythmias requiring drug or device therapy;

19. Any investigational drug within 30 days or five half-lives (whichever is longer)
   preceding the first dose of SB-485232;

20. The subject has active signs of a bowel obstruction.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study


Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Cancer Clinical Trials Office
Not Recruiting